Large-scale genomics unveil polygenic architecture of human cortical surface area

dc.contributor.authorChen, Chi-Hua
dc.contributor.authorPeng, Qian
dc.contributor.authorSchork, Andrew J.
dc.contributor.authorLo, Min-Tzu
dc.contributor.authorFan, Chun-Chieh
dc.contributor.authorWang, Yunpeng
dc.contributor.authorDesikan, Rahul S.
dc.contributor.authorBettella, Francesco
dc.contributor.authorHagler, Donald J.
dc.contributor.authorWestlye, Lars T.
dc.contributor.authorKremen, William S.
dc.contributor.authorJernigan, Terry L.
dc.contributor.authorHellard, Stephanie Le
dc.contributor.authorSteen, Vidar M.
dc.contributor.authorEspeseth, Thomas
dc.contributor.authorHuentelman, Matt
dc.contributor.authorHåberg, Asta K.
dc.contributor.authorAgartz, Ingrid
dc.contributor.authorDjurovic, Srdjan
dc.contributor.authorAndreassen, Ole A.
dc.contributor.authorSchork, Nicholas
dc.contributor.authorDale, Anders M.
dc.contributor.departmentDepartment of Radiology and Imaging Sciences, IU School of Medicineen_US
dc.date.accessioned2016-03-18T20:18:16Z
dc.date.available2016-03-18T20:18:16Z
dc.date.issued2015-07-20
dc.description.abstractLittle is known about how genetic variation contributes to neuroanatomical variability, and whether particular genomic regions comprising genes or evolutionarily conserved elements are enriched for effects that influence brain morphology. Here, we examine brain imaging and single-nucleotide polymorphisms (SNPs) data from ~2,700 individuals. We show that a substantial proportion of variation in cortical surface area is explained by additive effects of SNPs dispersed throughout the genome, with a larger heritable effect for visual and auditory sensory and insular cortices (h2~0.45). Genome-wide SNPs collectively account for, on average, about half of twin heritability across cortical regions (N=466 twins). We find enriched genetic effects in or near genes. We also observe that SNPs in evolutionarily more conserved regions contributed significantly to the heritability of cortical surface area, particularly, for medial and temporal cortical regions. SNPs in less conserved regions contributed more to occipital and dorsolateral prefrontal cortices.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationChen, C.-H., Peng, Q., Schork, A. J., Lo, M.-T., Fan, C.-C., Wang, Y., … Dale, A. M. (2015). Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature Communications, 6, 7549. http://doi.org/10.1038/ncomms8549en_US
dc.identifier.issn2041-1723en_US
dc.identifier.urihttps://hdl.handle.net/1805/8948
dc.language.isoen_USen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionof10.1038/ncomms8549en_US
dc.relation.journalNature Communicationsen_US
dc.rightsAttribution 3.0 United States
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/
dc.sourcePublisheren_US
dc.subjectpolymorphismen_US
dc.subjectnucleotidesen_US
dc.subjectgenomicsen_US
dc.subjectPolymorphism, Single Nucleotideen_US
dc.subjectcortexesen_US
dc.subjectgenomeen_US
dc.subjectgenesen_US
dc.subjectbrainen_US
dc.titleLarge-scale genomics unveil polygenic architecture of human cortical surface areaen_US
dc.typeArticleen_US
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